Vaccines-Autism Link *Not* an "Elaborate Fraud" - it's the same Chronic-Fatigue/Lyme link (immunosuppression)
Kathleen
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Subject: Vaccines-Autism Link *Not* an "Elaborate Fraud" - it's the
same Chronic-Fatigue/Lyme link (immunosuppression)
Date: Jan 6, 2011 2:10 AM
Non-science Article Below
===================================
No.
1) Children who are immune compromised
by fungal antigens (Is there not an epidemic
of asthma among children? The immune
-suppression outcome is its polar opposite)
http://www.actionlyme.org/101016.htm
should get fully heat-killed vaccines:
"Measles, mumps, and rubella--vaccine use and strategies for
elimination of measles, rubella, and congenital rubella syndrome and
control of mumps: recommendations of the Advisory Committee on
Immunization Practices (ACIP)."
http://www.ncbi.nlm.nih.gov/pubmed/9639369
"Changes in the recommended interval between administration of immune
globulin and measles vaccination; and Updated information on adverse
events and contraindications, particularly for persons with severe HIV
infection, persons with a history of egg allergy or gelatin allergy,
persons with a history of thrombocytopenia, and persons receiving
steroid therapy."
2) The gut-story has some basis in the same
scientific reality. Notice irritable bowel
(a symptom of FibroFeminoFatigue Lyme) is
treated with antibiotics:
http://www.dailymail.co.uk/health/article-1344560/A-possible-relief-pain-irritable-bowel-syndrome-Study-shows-antibiotic-used-treat-travellers-stomach-bugs-help.html?ito=feeds-newsxml
So, Wakefield was right, but for the
wrong reasons.
Let's stick to the science. The science
says that "Children with mitochondrial
disorders, as a result of fungal antigens
attaching to the mitochondrial membrane
http://www.actionlyme.org/101016.htm "
should be given fully heat killed viruses
and not attenuated viruses, because they
can't make the antibodies, because they
have this fungi stuck to the internal
workings of immune cells.
Once compromised in this way - like
with Pam3Cys-vaccination or hyperexposure
to moldy homes or whatever - these fungal
antigens are A) not recognized by the body
(tolerance) and B) suffer activated
latent (or acquired thru vaccination)
viruses due to the induced anti-apoptosis
genes.
Now, allow me to provide the reference on
that, because I did not, the last time:
http://www.actionlyme.org/GREATEST_IMITATOR_INTERVIEW.htm
"Meningococcal porin PorB prevents cellular apoptosis in a toll-like
receptor 2- and NF-kappaB-independent manner." PubMed ID:
"Meningococcal porin PorB is an inhibitor of apoptosis induced via the
intrinsic pathway in various cell types. This effect is attributed to
prevention of mitochondrial depolarization and of subsequent release
of proapoptotic mitochondrial factors. To determine whether apoptosis
is globally inhibited by PorB, we compared the intrinsic and extrinsic
pathways in HeLa cells. Interestingly, PorB does not prevent extrinsic
apoptosis induced by tumor necrosis factor alpha plus cycloheximide,
suggesting a unique mitochondrial pathway specificity. Several
intracellular factors regulated by NF-kappaB, including members of the
Bcl-2 family and of the inhibitor of apoptosis (IAP) family, play
major roles in controlling apoptosis, and some of them are thought to
contribute to the antiapoptotic effect of the gonococcal porin, PIB.
However, most of the members of the Bcl-2 family and the IAP family
are not induced by meningococcal PorB in HeLa cells, with the
exception of Bfl-1/A1. Interestingly, PorB does not induce NF-kappaB
activation in HeLa cells, likely due to a lack of Toll-like receptor 2
(TLR2) expression in these cells. Bfl-1/A1 expression is also
regulated by CBF1, a nuclear component of the Notch signaling pathway,
independent of NF-kappaB activation. Since HeLa cells are protected by
PorB from intrinsic apoptosis events, regardless of TLR2 and NF-kappaB
expression, the possibility of a contribution of alternative signaling
pathways to this effect cannot be excluded. ***In this paper, we
describe an initial dissection of the cascade of cellular events
involved in the antiapoptotic effect of PorB in the absence of
TLR2.***
http://www.ncbi.nlm.nih.gov/pubmed/20028813
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825956/?tool=pubmed
The likes of OspA and fungal exposures
result, somehow, in the activation of
anti-apoptotic genes, like BCL2.
So, let's stick to the science and not
have "journalists" or anyone at Yale
or UConn interpreting it for us. We
all already know they've been completely
defunded and sued and lost Plum Island,...
and they're still screaming their Lyme
nonsense without ever having explained
to anyone what Pam3Cys is:
http://www.actionlyme.org/101016.htm
It *is* true that kids with fungal-immunosuppression
or genetically-acquired over-expression
of BCL2 class molecules will have bowel
problems. We all know kids with autism
have bowel problems, and we know people
with FibroFemino have bowel problems
because they pretty much can't handle
any infections on their own.
We just even saw Anthony Fauci talk
about a side-ways version of this:
http://www.businessweek.com/lifestyle/content/healthday/648087.html
"Federal researchers say they've gained insight into how to analyze
the risks facing people with a rare immune system-weakening condition
called chronic granulomatous disease, paving the way toward more
personalized treatment."
That's the second step he's taken
towards admitting that certain
malfunctions of immunity exist
after he admitted the *LYMErix*
could never have been a vaccine
against *HIV* because fungal antigens
SUPPRESS the immune system:
http://www.actionlyme.org/101016.htm
Now, start paying attention.
It happened to the child of a Johns
Hopkins MD. It could happen to your
own. Imagine spending the first
25 years of your child's life in
chronic *agony* over what's going
to happen to them in these State
institutions. We all know damned
well, that perverts are attracted
to this business:
http://www.actionlyme.org/RAGAGLIA_GRANDJURY_DETAILS.htm
KMDickson
http://www.actionlyme.org
http://www.relapsingfever.org
=============================================
http://www.cbsnews.com/stories/2011/01/05/health/main7217168.shtml
(AP) LONDON -- The first study to link a childhood vaccine to autism
was based on doctored information about the children involved,
according to a new report on the widely discredited research.
The conclusions of the 1998 paper by Andrew Wakefield and colleagues
was renounced by 10 of its 13 authors and later retracted by the
medical journal Lancet, where it was published. Still, the suggestion
the MMR shot was connected to autism spooked parents worldwide and
immunization rates for measles, mumps and rubella have never fully
recovered.
A new examination found, by comparing the reported diagnoses in the
paper to hospital records, that Wakefield and colleagues altered facts
about patients in their study.
The analysis, by British journalist Brian Deer, found that despite the
claim in Wakefield's paper that the 12 children studied were normal
until they had the MMR shot, five had previously documented
developmental problems. Deer also found that all the cases were
somehow misrepresented when he compared data from medical records and
the children's parents.
Wakefield could not be reached for comment despite repeated calls and
requests to the publisher of his recent book, which claims there is a
connection between vaccines and autism that has been ignored by the
medical establishment. Wakefield now lives in the U.S. where he enjoys
a vocal following including celebrity supporters like Jenny McCarthy.
Deer's article was paid for by the Sunday Times of London and
Britain's Channel 4 television network. It was published online
Thursday in the medical journal, BMJ.
In an accompanying editorial, BMJ editor Fiona Godlee and colleagues
called Wakefield's study "an elaborate fraud." They said Wakefield's
work in other journals should be examined to see if it should be
retracted.
Last May, Wakefield was stripped of his right to practice medicine in
Britain. Many other published studies have shown no connection between
the MMR vaccination and autism.
But measles has surged since Wakefield's paper was published and there
are sporadic outbreaks in Europe and the U.S. In 2008, measles was
deemed endemic in England and Wales.
KMDickson